Probiotics to Actively Counter Ventilator Associated Pneumonia (PROACT)

Sponsor

University of Bari (Other)

Overall Status

Not yet recruiting

CT.gov ID

NCT06092554

Collaborator

Uni-Pharma (Industry)

186

Enrollment

Locations

Arms

Anticipated Duration (Months)

Patients Per Site

5.2

Patients Per Site Per Month

Study Details

Study Description

Brief Summary

PROACT study aims to resolve uncertainties to influence actual practice guidelines or public health policing regarding VAP prevention in ICU by using probiotics administration.

Multi-trauma patients with a head injury OR stroke or brain haemorrhage patients without any sign of aspiration and lung infection will be enrolled and randomized to either placebo or probiotic treatment to assess if VAP and mortality can be reduced in the interventional group.

Condition or Disease	Intervention/Treatment	Phase
Ventilator Associated Pneumonia	Dietary Supplement: LactoLevure Other: Placebo	N/A

Detailed Description

Ventilator-associated pneumonia represents a burden in ICU with a mortality rate approaching 50%. Ventilator-associated pneumonia (VAP) reduction care bundle is a grouping of evidence-based, high-impact interventions.

Among these recommendations:

raised head of bed (minimizes microaspiration)
daily sedation hold and assessment of readiness to extubate (decreases length of stay)
use of subglottic secretion drainage
avoidance of scheduled ventilator circuit changes
peptic ulcer prophylaxis (minimizes complications and length of stay)
venous thrombo-embolism prophylaxis (minimizes complications and length of stay) Probiotics administration does not figure yet in these recommendations despite the literature showing interesting results in VAP reduction, particularly in specific subsets of patients such as trauma. Tsilika et al. demonstrated a VAP reduction in trauma patients with a head injury. The incidence was lowered to 11.9% in the interventional group with a four-probiotic preparation administration from 28.3 % in the placebo group. The same probiotic preparation has been used in multiple trauma patients to reduce surgical site infections, supporting a possibly prophylactic administration of probiotics. A different two-probiotic preparation was given in stroke patients and showed a VAP incidence reduction in the probiotic group. Stroke patients and trauma patients with a head injury share a common pathophysiology, as traumatic brain injury is considered a risk factor for stroke.

Recent reviews and meta-analyses suggest that probiotics administration may reduce VAP incidence, but more studies with a higher level of evidence and low bias are warranted. The rationale for this finding is yet to be understood. Still, it might depend on the communications between the Gut microbiota (GM) and the oral microbiota (OM) on one side and the lung and its microbiota on the other, along the gut-lung and the gut-bone marrow-lung axes. Notably, short-chain fatty acids (SCFAs) such as butyrate, acetate and propionate produced by the GM by fibre fermentation may have anti-inflammatory effects that strengthen the respiratory tract's epithelial barrier. Tailored and early probiotic administration in the critically ill patient when he enters the ICU, may positively modulate the GM and protect the patient from the harmful downside of the GM disruption. The GM imbalance, called dysbiosis, occurs within six hours of ICU admission, leading to lower bacterial diversity and variability while opportunistic pathogens take over symbiotics. Disrupting this vicious cycle which transforms the local GM into a pathobiota, may play a key role in preserving the good functioning of the gut-lung axis. The diversity of the results of published Randomized Controlled Trials (RCT) guiding the necessity for meta-analysis is probably coming from the heterogeneity of the studied patient population and one inclusion bias: it seems that for probiotics to act prophylactically, the enrolled patient population should be as much as possible devoid of any infection. Indeed a recent large-scale RCT from Canada failed to show any benefit of probiotic treatment to reduce the incidence of VAP. However, most participants were already on antibiotics for unspecific infections, and the methods lacked microbiology diagnosis to support VAP detection.

PROACT is a double-blind randomized placebo-controlled clinical trial where the effect of a four probiotic preparation (Lactolevure, Unipharma, Greece) is studied on multi-trauma patients with a head injury OR stroke or brain haemorrhage patients without any sign of aspiration and lung infection to assess whether this supplementation can reduce VAP and mortality.

Patients eligible for enrollment are admitted to the hospital from the emergency department or transferred from another ICU. A legal representative will be asked for written informed consent once a patient classifies as acute brain trauma, stroke, or brain hemorrhage patient. Therefore, eligibility screening can start, and exclusion criteria will first be assessed. If the patient does not meet any exclusion criteria, he will also be considered for inclusion criteria. If the patient meets all the inclusion criteria, he can be successfully enrolled in the study.

The patient will be blindly assigned at a 1:1 ratio to either the interventional (probiotics) group or the control ( placebo) group.

The research coordinator and the sub-investigators will assess patients daily in the ICU, where most data will be gathered. The investigators and the clinicians evaluating the patients will be blind to the allocated treatment for the entire study duration.

This includes:

Baseline data: demographics (age, gender, height, weight, country of origin), total comorbidities number on admission, cardiovascular axis on admission, pulmonary axis on admission, metabolic axis on admission, liver axis on admission, rheumatic axis on admission, renal axis on admission, neurologic axis on admission, history of smoking, Glasgow Coma Scale (GCS) on admission, sequential organ failure assessment (SOFA) score on admission, Acute Physiology and Chronic Health Evaluation (APACHE II) score on admission, Simplified Acute Physiology Score (SAPS) II score on admission, Charlson Comorbidity Index. Before start of the study drug, one sample of tracheobronchial secretions will be collected and analyzed quantitatively. This step is necessary to define the modified intention-to-treat (mITT) population.
Daily data: vital signs, sepsis, septic shock, CRBSI, Catecholamine support, Enteral feeding, Parenteral feeding, Enteral + Parenteral feeding, prokinetics, beta-lactamase inhibitor, second-generation cephalosporin, third-generation cephalosporin, piperacillin/tazobactam, metronidazole, clindamycin, amikacin, glycopeptide, microbiology and antibiogram (if available), GCS score, SOFA score, diarrhoea (type 6/7 bristol stool chart), mechanical ventilation, Oxygen saturation (SpO2), culture results, adverse events.
VAP screening: every day, the patient will be screened explicitly for VAP by the attending physician. The screening protocol begins with clinical suspicion. The presence of new or progressive radiographic infiltrates and at least two of three clinical criteria [19] ( fever/hypothermia, leukocytosis/leukopenia, purulent secretions) represent the protocol trigger. Leukocytosis is defined as an elevation in the absolute White Blood Cells (WBC) count (10,000 cells/μL), while leukopenia is defined as a reduction in the WBC count (<3500 cells/μL) [20]. Hypothermia is defined as a body core temperature of <35.0 °C (95.0 °F) [21], while fever is defined as a body core temperature of ≥38.3°C (101° F) [22]. Once the clinical suspicion is realized, samples of respiratory secretions, i.e. tracheal aspirate and bronchoalveolar lavage (BAL), are obtained non-invasively. Samples will be quantitatively cultured at the local hospital laboratory. Part of the samples will be stored at -20 °C and shipped by air transport to the Laboratory of Immunology of Infectious Diseases of the 4th Department of Internal Medicine of ATTIKON University General Hospital (124 62 Athens, Greece) for molecular testing. A VAP diagnosis will be established if either quantitative cultures yield more than 105 cfu/ml growth of one pathogen or when more than 104 copies of a pathogen are grown in molecular testing.

FOLLOW-UP: The data collection will continue for at least 30 days unless the patient is successfully extubated, interrupting mechanical ventilation. In this case, the data collection and the probiotic administration will continue for 72 hours after successful weaning to pass the time window for a late VAP diagnosis. The data collection will continue for two additional days if a patient is still in the ICU after the thirtieth day until discharge, although the intervention stops. If VAP is diagnosed, the patient will continue the probiotic administration for up to 30 days as per the study protocol since there may still be a beneficial effect on the secondary outcomes.

Biological samples will be collected pre- and post-treatment (after 30 days or 72h after successful extubation) to study how probiotics administration affects GM's composition. The samples are going to be faeces, blood and urine.

Study Design

Study Type:

Interventional

Anticipated Enrollment :

186 participants

Allocation:

Randomized

Intervention Model:

Parallel Assignment

Intervention Model Description:

The present study will be a multicenter, randomized, double-blind, placebo-controlled trial. Allocation will rely on a computer-based random number generator provided in a sequentially numbered, sealed, opaque envelope.The present study will be a multicenter, randomized, double-blind, placebo-controlled trial. Allocation will rely on a computer-based random number generator provided in a sequentially numbered, sealed, opaque envelope.

Masking:

Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

Masking Description:

A numbered sealed envelope will be used to ensure blinding.

Primary Purpose:

Prevention

Official Title:

Probiotics in ICU to Reduce Ventilator-Associated Pneumonia: A Double-blind Multicentre Randomized Clinical Trial

Anticipated Study Start Date :

Nov 15, 2023

Anticipated Primary Completion Date :

May 15, 2025

Anticipated Study Completion Date :

May 15, 2025

Arms and Interventions

Arm	Intervention/Treatment
Experimental: Interventional: Probiotics Patients will receive a four probiotic preparation (LactoLevure, UniPharma, Athens, Greece).) in capsules containing: Lactobacillus acidophilus LA-5 [1.75 × 109 colony-forming units (cfu)], Lactobacillus plantarum (0.5 × 109 cfu), Bifidobacterium lactis BB12 (1.75 × 109 cfu) and Saccharomyces boulardii (1.5 × 109 cfu).	Dietary Supplement: LactoLevure Patients will receive two capsules, twice daily for 30 days, one through the nasogastric tube and one spread on the oropharynx. The probiotic capsules look identical to the placebo capsules; the powder will be similar when opened. The capsule for nasogastric tube will be opened and suspended in 100 ml of tap water. The capsule for the oropharynx will be opened and suspended in sterile water based surgical lubricant. The administration must happen at least 30 minutes after oral antiseptic product usage (e.g. daily chlorhexidine oral care), which otherwise might neutralize the study supplement's action.
Placebo Comparator: Control: Placebo Patients will receive a placebo in capsules containing powdered glucose polymer.	Other: Placebo Patients will receive two capsules, twice daily for 30 days, one through the nasogastric tube and one spread on the oropharynx. The placebo capsules contain a powdered glucose polymer that is unharmful for the patient and will be provided by the sponsor. The placebo capsules look identical to the probiotic capsules; the powder will be similar when opened. The capsule for nasogastric tube will be opened and suspended in 100 ml of tap water. The capsule for the oropharynx will be opened and suspended in sterile water based surgical lubricant. The administration must happen at least 30 minutes after oral antiseptic product usage (e.g. daily chlorhexidine oral care), which otherwise might neutralize the study supplement's action.

Arm

Intervention/Treatment

Experimental: Interventional: Probiotics

Patients will receive a four probiotic preparation (LactoLevure, UniPharma, Athens, Greece).) in capsules containing: Lactobacillus acidophilus LA-5 [1.75 × 109 colony-forming units (cfu)], Lactobacillus plantarum (0.5 × 109 cfu), Bifidobacterium lactis BB12 (1.75 × 109 cfu) and Saccharomyces boulardii (1.5 × 109 cfu).

Dietary Supplement: LactoLevure

Patients will receive two capsules, twice daily for 30 days, one through the nasogastric tube and one spread on the oropharynx. The probiotic capsules look identical to the placebo capsules; the powder will be similar when opened. The capsule for nasogastric tube will be opened and suspended in 100 ml of tap water. The capsule for the oropharynx will be opened and suspended in sterile water based surgical lubricant. The administration must happen at least 30 minutes after oral antiseptic product usage (e.g. daily chlorhexidine oral care), which otherwise might neutralize the study supplement's action.

Placebo Comparator: Control: Placebo

Patients will receive a placebo in capsules containing powdered glucose polymer.

Other: Placebo

Patients will receive two capsules, twice daily for 30 days, one through the nasogastric tube and one spread on the oropharynx. The placebo capsules contain a powdered glucose polymer that is unharmful for the patient and will be provided by the sponsor. The placebo capsules look identical to the probiotic capsules; the powder will be similar when opened. The capsule for nasogastric tube will be opened and suspended in 100 ml of tap water. The capsule for the oropharynx will be opened and suspended in sterile water based surgical lubricant. The administration must happen at least 30 minutes after oral antiseptic product usage (e.g. daily chlorhexidine oral care), which otherwise might neutralize the study supplement's action.

Outcome Measures

Primary Outcome Measures

Vap Incidence [45 days]
VAP is defined as first episode of lower respiratory tract infection that meets all the following criteria: (a) onset >48 h after initiation of mechanical ventilation; (b) increase in SOFA score by ≥1 point; (c) new infiltrate in chest X-ray or chest computed tomography; (d) core temperature >38°C; (e) purulent tracheobronchial secretions; (f) clinical pulmonary infection score (CPIS) >6 ; and (g) isolation of a pathogen from BAL fluid (>1 × 104 cfu/mL) or tracheal aspirate (>1 × 105 cfu/mL) . This is analyzed for the ITT population. The ITT comprises the total of enrolled and randomized patients.

Secondary Outcome Measures

Vap incidence analyzed for mITT [45 days]
The mITT comprised only patients with less than 102 cfu/ml of bacterial growth in tracheobronchial secretions before start of the study drug.
Sepsis [45 days]
Sepsis is defined as a new infection with at least a 2-point increase in the total SOFA score. The endpoint will be analyzed for both the ITT and mITT populations.
Septic shock [45 days]
Septic shock is defined as sepsis aggravated by hypotension and serum lactate level >2 mmol/L (18 mg/dL) that requires vasopressors administration despite adequate volume resuscitation. The endpoint will be analyzed for both the ITT and mITT populations.
Catheter-related bloodstream infections (CRBSI) [45 days]
CRBSI, according to the Infectious Diseases Society of America, is defined when one of the following criteria is met 1) Isolation of the same pathogen from a quantitative blood culture drawn through the central line and from a peripheral vein with the single bacterial colony count at least threefold higher in the sample from the central line as compared to that obtained from a peripheral vein 2) same organism recovered from percutaneous blood culture and from quantitative (>15 colony-forming units) culture of the catheter tip 3) a shorter time to positive culture (>2 hours earlier) in the central line sample than the peripheral sample (differential time to positivity [ DTP ]). The endpoint will be analyzed for both the ITT and mITT populations.
ICU length of stay [45 days]
Duration in days of the patient stay in the ICU. The endpoint will be analyzed for both the ITT and mITT populations.
Mechanical ventilation days [45 days]
Mechanical ventilation days is to be intended as the total number of days during which the patient underwent mechanical ventilation. The endpoint will be analyzed for both the ITT and mITT populations.

Eligibility Criteria

Criteria

Ages Eligible for Study:

18 Years to 80 Years

Sexes Eligible for Study:

All

Accepts Healthy Volunteers:

Inclusion Criteria:

adults aged 18-80 years
at least one of the following conditions: a) recent trauma involving head injury and at least one more organ system; b) stroke or brain hemorrhage without any sign of aspiration and lung infection
intubation and start of mechanical ventilation. This needs to start immediately after the event described in the inclusion criteria (b). For cases of head trauma this is defined as start in the ambulance or the emergency department
likelihood that the duration of mechanical ventilation would be at least six days
written informed consent provided by the patient or legal representative

Exclusion Criteria:

has received mechanical ventilation more than 72 hours from start of screening
pregnancy or Lactation
patients at risk of iatrogenic probiotic infection e.g. immunosuppression which includes
HIV <200 CD4 cells/μL
those receiving chronic immunosuppressive medications (e.g., azathioprine, cyclosporine, cyclophosphamide, tacrolimus, methotrexate, mycofenolate, Anti-IL2)
previous transplantation at any time
malignancy requiring chemotherapy in the last 3 months
neutropenia [absolute neutrophil count < 500])
patients with a primary diagnosis of severe pancreatitis (Ranson score of 3 or more). Mild and moderate pancreatis is not excluded
ischemic bowel disease
oropharyngeal mucosal injury
inability to receive enteral medications
intent to withdraw advanced life support as per ICU doctor in charge
patients at risk of endovascular infection which includes

previously documented rheumatic heart disease, congenital valve disease, surgically repaired congenital heart disease, unrepaired cyanotic congenital heart disease, any intracardiac repair with prosthetic material [mechanical or bioprosthetic cardiac valves]
previous or current endocarditis
permanent endovascular devices (e.g., endovascular grafts [e.g., aortic aneurysm repair, stents involving large arteries such as aorta, femorals and carotids] inferior vena cava filters, dialysis vascular grafts
tunnelled (not short-term) hemodialysis catheters
pacemakers or defibrillators

Patients with peripherally inserted central catheters (PICCs), temporary central venous catheters, central venous dialysis catheters, coronary artery stents, coronary artery bypass grafts (CABG), or neurovascular coils are not excluded, nor are patients with mitral valve prolapse or bicuspid aortic valve if they do not meet any other exclusion criteria.